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PUREMED Sterile Endoscopic Biopsy Needles - Indonesia BPOM Medical Device Registration

PUREMED Sterile Endoscopic Biopsy Needles is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801420027. The device is manufactured by PUREMED PRODUCTS (YANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. AIR THEN PHARMA.

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BPOM Registered
Risk Class Kelas Resiko : B
PUREMED Sterile Endoscopic Biopsy Needles
Analysis ID: AKL 20801420027

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. AIR THEN PHARMA

AR Address

Citra Towers, North Tower Lantai 10 Unit 10A, Jalan Benyamin Suaeb Kavling A6

Registration Date

Jan 16, 2024

Expiry Date

Dec 31, 2025

Product Type

Diagnostic Gastroenterology-Urology Equipment

Gastroenterology-urology biopsy instrument

Non Electromedic Sterile

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